MEIJI Co., Ltd. - OSAKA FACTORY
FDA import alert and refusal historyTakatsuki, JapanFEI 3004252918
As of October 26, 2026, MEIJI Co., Ltd. - OSAKA FACTORY is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on March 8, 2017, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Protein component, infant formula raw material component · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for MEIJI Co., Ltd. - OSAKA FACTORY
5 records, newest first. Each line links to the FDA page it came from.
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2017
- Import refusalSource
Refused, 3 lines in one entry: Protein component, infant formula raw material component; Granola bars and 1 moreNO ENGLISHNUTRIT LBLNCONTACTEntry UPS-2172837-4Show 3 linesHide lines
- Refused, Protein component, infant formula raw material componentNO ENGLISHNUTRIT LBLEntry UPS-2172837-4Source
- Refused, Granola barsNO ENGLISHNUTRIT LBLEntry UPS-2172837-4Source
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHNCONTACTNUTRIT LBLEntry UPS-2172837-4Source
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Refusal charges, in plain English
- NO ENGLISH3 refused lines
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
- NUTRIT LBL3 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- NCONTACT1 refused line
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
Questions about MEIJI Co., Ltd. - OSAKA FACTORY
- Is MEIJI Co., Ltd. - OSAKA FACTORY on an FDA import alert?
- No listing for MEIJI Co., Ltd. - OSAKA FACTORY appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from MEIJI Co., Ltd. - OSAKA FACTORY?
- Yes. FDA refused 3 shipment lines from MEIJI Co., Ltd. - OSAKA FACTORY on March 8, 2017. The most recent, on March 8, 2017, was protein component, infant formula raw material component, charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse MEIJI Co., Ltd. - OSAKA FACTORY's shipments?
- The most frequent charges are NO ENGLISH (required label information not in english, 3 lines) and NUTRIT LBL (nutrition information missing from label, 3 lines).
- When was MEIJI Co., Ltd. - OSAKA FACTORY last inspected by FDA?
- FDA's most recent inspection of MEIJI Co., Ltd. - OSAKA FACTORY with a final classification is dated August 2, 2018 and was classified NAI (No Action Indicated).
- What is MEIJI Co., Ltd. - OSAKA FACTORY's FEI number?
- MEIJI Co., Ltd. - OSAKA FACTORY's FDA Establishment Identifier (FEI) is 3004252918.
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